# KITRON AB

FEI: 3009834076
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: Kitron AB (#10042519)

Address: Mobelvagen 5, Jonkoping, SE-55652, SE

Mandatory US Agent: FDA Agent Pro LLC

## Products

Total registered: 1
Top product codes: JOY
Regulation §: 864.5260

Proprietary names: CellaVision DC-1

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223009834076%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3009834076